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Senyawa ini adalah salah satu dari beberapa [[isomer]] [[amil alkohol]]. Cairan nirwarna ini terjadi secara alami dalam jumlah kecil dan telah menarik perhatian sebagai [[bahan bakar hayati]] yang potensial, dengan memanfaatkan sifat hidrofobik (seperti bensin) dan struktur bercabangnya. Ia adalah molekul [[kiralitas|kiral]].<ref>{{cite journal |doi=10.1002/1521-3773(20011203)40:23<4422::AID-ANIE4422>3.0.CO;2-G|title=Enantioseparation of Racemic Organic Molecules by a Zeolite Analogue|year=2001|last1=Xiong|first1= Ren-Gen|last2=You|first2=Xiao-Zeng|last3=Abrahams|first3= Brendan F.|last4=Xue|first4=Ziling|last5=Che|first5=Chi-Ming|journal=Angewandte Chemie International Edition|volume=40|issue=23|pages=4422–4425|pmid=12404434}}</ref> ==Kemunculan== 2-Metil-1-butanol adalah komponen dari banyak campuran [[amil alkohol]] komersial. Senyawa ini adalah salah satu dari banyak komponen aroma berbagai jamur dan buah, misalnya [[truffle]] musim panas, tomat,<ref>{{cite journal |doi=10.1021/jf00076a025|title=Fresh tomato aroma volatiles: A quantitative study|year=1987|last1=Buttery|first1=Ron G.|last2=Teranishi|first2=Roy|last3=Ling|first3=Louisa C.|journal=Journal of Agricultural and Food Chemistry|volume=35|issue=4|pages=540–544}}</ref> dan [[blewah]].<ref>{{cite journal |doi=10.1016/j.chroma.2003.08.016|title=Truffle Aroma Characterization by Headspace solid-phase microextraction|year=2003|last1=Dı́Az|first1=P.|last2=Ibáñez|first2 =E.|last3=Señoráns|first3=F.J|last4=Reglero|first4=G.|journal=Journal of Chromatography A|volume=1017|issue=1–2|pages=207–214|pmid=14584705}}</ref><ref>{{cite journal |doi=10.1021/jf0005768|title=Identification of Volatile Compounds in Cantaloupe at Various Developmental Stages Using Solid Phase Microextraction|year=2001|last1=Beaulieu|first1=John C.|last2=Grimm|first2=Casey C.|journal=Journal of Agricultural and Food Chemistry|volume=49|issue=3|pages=1345–1352|pmid=11312862}}</ref> ==Produksi dan reaksi== 2-Metil-1-butanol telah diproduksi dari glukosa oleh [[Escherichia coli|E. coli]] yang dimodifikasi secara genetik. 2-Keto-3-metilvalerat, prekursor [[treonina]], diubah menjadi alkohol target melalui aksi berurutan dari asam 2-keto, [[karboksi-liase|dekarboksilase]] dan [[dehidrogenase]].<ref>{{cite journal |doi=10.1038/nature06450|title=Non-Fermentative Pathways for Synthesis of Branched-Chain Higher Alcohols as Biofuels|year=2008|last1=Atsumi|first1=Shota|last2= Hanai|first2=Taizo|last3=Liao|first3=James C.|journal=Nature|volume=451|issue=7174|pages=86–89|pmid=18172501|bibcode=2008Natur.451...86A|s2cid=4413113}}</ref> Ia dapat berasal dari [[alkohol fusel|minyak fusel]] (karena terjadi secara alami pada [[buah|buah-buahan]] seperti [[anggur]]<ref name="hef"> {{Citation | last = Howard | first = Philip H. | year = 1993 | title = Handbook of Environmental Fate and Exposure Data for Organic Chemicals | volume = 4 | publication-place = Boca Raton, Florida | publisher = CRC Press | isbn = 978-0-87371-413-6 | pages = 392–396 | url = https://books.google.com/books?id=HdhohbQrg8IC&pg=PA392 | access-date = 25 Januari 2024 }}</ref>) atau diproduksi melalui [[Hidroformilasi|proses okso]] atau [[halogenasi]] [[pentana]].<ref name="encyc" /> ==Lihat pula== * [[Tert-Amil alkohol|2-Metil-2-butanol]] ==Referensi== {{Reflist}} {{Alkohol}} {{DEFAULTSORT:Metil-1-butanol, 2-}} [[Kategori:Alkanol]] [[Kategori:Alkohol lemak]] [[Kategori:Alkohol primer]] </textarea><div class="templatesUsed"><div class="mw-templatesUsedExplanation"><p>Templat yang digunakan di halaman ini: </p></div><ul> <li><a href="/wiki/Templat:Abbr" title="Templat:Abbr">Templat:Abbr</a> (<a href="/w/index.php?title=Templat:Abbr&action=edit" title="Templat:Abbr">lihat sumber</a>) (semi-dilindungi)</li><li><a href="/wiki/Templat:Alkohol" 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